Trifluoroacetic acid → 5-Bromo-6-cyclopropyl-3-iodopyridin-2-amine
反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH2:11])=[N:6][C:7]=1[CH:8]1[CH2:10][CH2:9]1.FC(F)(F)C(O)=O.[I:19]N1C(=O)CCC1=O>>[Br:1][C:2]1[CH:3]=[C:4]([I:19])[C:5]([NH2:11])=[N:6][C:7]=1[CH:8]1[CH2:9][CH2:10]1参加物
4
実験手順
A solution of 5-bromo-6-cyclopropylpyridin-2-amine (2.1 g, 9.81 mmol), trifluoroaceticacid (170 mg, 1.47 mmol), N-iodosuccinimide (2.2 g, 9.81 mmol) stirred at room temperature for 30 minutes. Reaction mass was quenched with water, basified with ammonium hydroxide solution. Solid separated was filtered and dried to get 3.3 g (100% yield) of titled compound. 1H NMR (CDCl3, 300 MHz): δ 7.85 (s, 1H), 4.80-4.65 (bs, 2H), 2.39-2.25 (m, 1H), 1.0-0.90 (m, 4H). MS: m/z=338.9 (M+1).
後処理
- customReaction mass
- customwas quenched with water
- customSolid separated
- filtrationwas filtered
- customdried
出典と根拠
- ORDレコード
- ord-1964b8422f8c46aebd9ca5d09c80cde2
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09353107B2
反応ノート
読み込み中…